131268-46-7

Basic information

• Product Name: 9,10-Anthracenedione, 2,6-diphenyl-
• CAS NO: 131268-46-7
• Molecular Formula: C26H16O2
• Molecular Weight: 360.412
• Mol File: 131268-46-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 9,10-Anthracenedione, 2,6-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 9,10-Anthracenedione, 2,6-diphenyl-(131268-46-7)
• EPA Substance Registry System: 9,10-Anthracenedione, 2,6-diphenyl-(131268-46-7)

Safety Data

• Hazardous Substances Data: 131268-46-7(Hazardous Substances Data)

Upstream product

• 24388-23-6 2-phenyl-4,4,5,5-tetramethyl-1,3,2-dioxoborole 
• 131559-19-8 bistriflate of 2,6-dihydroxy-9,10-anthraquinone 
• 98-80-6 phenylboronic acid 
• 84-60-6 anthraflavic acid 
• 955-16-8 3,4-biphenyldicarboxylic anhydride 
• 92-52-4 biphenyl 
• 131-14-6 2,6-diamino-9,10-anthraquinone 
• 78507-46-7 2,6-diiodoanthracene-9,10-dione 
• 633-70-5 2,6-dibromoanthraquinone 

Downstream Products

• 84652-71-1 11,11,12,12-tetracyano-(2,6-diphenyl)-9,10-anthraquinodimethane 

Relevant articles and documents

Heteroarylation of anthraquinone-triflate by Suzuki cross-coupling

The reactivity of the 4-pyridylboronate 5a for PdCl2(dppf)catalysed cross-coupling reaction with an anthraquinone triflate is presented, and compared with its 2-thienyl- and phenylboronic analogues. Best results have been obtained on a small sc

2,6-Diaryl-9,10-anthraquinones as models for electron-accepting polymers

Anthraquinone derivatives have been little used in microelectronics though they are attractive scaffolds due to their electron-accepting properties. As part of a preliminary study, a series of conjugated anthraquinone derivatives has been synthesised. The

ANTHRACENE DERIVATIVES AND ORGANIC ELECTROLUMINESCENT DEVICES MADE BY USING THE SAME

An anthracene derivative represented by the following general formula (1) which enables an organic electroluminescence device to exhibit a great efficiency of light emission and uniform light emission even at high temperatures since crystallization is suppressed and no thermal decomposition takes place during vapor deposition and an organic electroluminescence device utilizing the derivative, are provided. [Ar represents a group represented by the following general formula (2): (L1 and L2 each represent a substituted or unsubstituted methylene group, ethylene group or the like, and at least one of them is present), Ar' represents a substituted or unsubstituted aryl group having 6 to 50 nuclear carbon atoms, X represent an alkyl group or the like, a and b each represent an integer of 0 to 4, and n represents an integer of 1 to 3.]